Evidence map›Paper›PMID 37736101›Full record

ArticleFrontiers in immunology2023

Allogeneic cord blood regulatory T cells decrease dsDNA antibody and improve albuminuria in systemic lupus erythematosus.

Mi-Ae Lyu, Ximing Tang, Joseph D Khoury, Maria Gabriela Raso, Meixian Huang, Ke Zeng, Mitsutaka Nishimoto, Hongbing Ma, Tara Sadeghi, Christopher R Flowers and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Review
  3. CD8Frontiers in immunology · 2026
    Review
  4. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Mi-Ae LyuDepartment of Lymphoma/Myeloma, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States.
Ximing TangDepartment of Translational Molecular Pathology, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States.
Joseph D KhouryDepartment of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States.
Maria Gabriela RasoDepartment of Translational Molecular Pathology, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States.
Meixian HuangDepartment of Lymphoma/Myeloma, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States.
Ke ZengDepartment of Lymphoma/Myeloma, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States.
Mitsutaka NishimotoDepartment of Lymphoma/Myeloma, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States.
Hongbing MaDepartment of Lymphoma/Myeloma, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States.
Tara SadeghiCellenkos Inc., Houston, TX, United States.
Christopher R FlowersDepartment of Lymphoma/Myeloma, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States.
Simrit ParmarDepartment of Lymphoma/Myeloma, The University of Texas M.D. Anderson Cancer Center, Houston, TX, United States.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIANE BODURKA · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Background: Lupus nephritis (LN) constitutes the most severe organ manifestations of systemic lupus erythematosus (SLE), where pathogenic T cells have been identified to play an essential role in 'helping' B cells to make autoantibodies and produce inflammatory cytokines that drive kidney injury in SLE. Regulatory T cells (Tregs), responsible for decreasing inflammation, are defective and decreased in SLE and have been associated with disease progression. We hypothesize that treatment with allogeneic, healthy Tregs derived from umbilical cord blood (UCB) may arrest such an inflammatory process and protect against kidney damage. Methods: UCB-Tregs function was examined by their ability to suppress CellTrace Violet-labeled SLE peripheral blood mononuclear cells (PBMCs) or healthy donor (HD) conventional T cells (Tcons); and by inhibiting secretion of inflammatory cytokines by SLE PBMCs. Humanized SLE model was established where female Rag2 Results: Conclusions: UCB-Tregs can decrease inflammatory burden in SLE, reduce auto-antibody production and resolve end organ damage especially, improve kidney function. Adoptive therapy with UCB-Tregs should be explored for treatment of lupus nephritis in the clinical setting.

Indexed as

Hematopoietic Stem Cell TransplantationLupus Erythematosus, SystemicLupus NephritisAlbuminuriaAnimalsAntibodies, AntinuclearCytokinesDNAFemaleFetal BloodHumansInflammationLeukocytes, MononuclearMiceT-Lymphocytes, RegulatoryAntibodies, AntinuclearCytokinesDNAalbuminuriaallogeneicdsDNA antibodieslupus nephritis (LN)regulatory T cells (Tregs)systemic lupus erythematosus (SLE)umbilical cord blood (UCB)

Identifiers

PMID37736101
PMCPMC10509479
OpenAlexW4386440515

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.